IP Library Granted Patent US 10,695,420
Granted Patent B2
US 10,695,420 · App. 15/528,502 · Granted Jun 30, 2020

DNA-peptide combination vaccine

Inventors: Hironori Nakagami (Suita, JP); Ryuichi Morishita (Suita, JP); Hiroshi Koriyama (Suita, JP); Hideki Tomioka (Ibaraki, JP); Kenji Naohara (Osaka, JP)
Assignees: ANGES, INC.; OSAKA UNIVERSITY; DS PHARMA ANIMAL HEALTH CO., LTD.
A61K39/292A61K39/0008C12N7/00A61K2039/53A61K2039/545A61K2039/70C12N2730/10134
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,695,420
App. No.
15/528,502
Granted
Jun 30, 2020
Kind
B2
Abstract

The present invention provides a combination preparation for inducing a specific immune response to an antigenic peptide, which contains (I) the antigenic peptide, and (II) an expression vector encoding a chimeric hepatitis B virus core antigen polypeptide, into which the antigenic peptide has been inserted or added, wherein said antigenic peptide is inserted in a region of amino acid residues 74-87 or 130-138 of the hepatitis B virus core antigen polypeptide, or added to the N-terminal or C-terminal of the hepatitis B virus core antigen polypeptide, wherein the antigenic peptide of (I) and the expression vector of (II) are substantially simultaneously administered to a subject.

Claims (22)

1. A combination for inducing a specific immune response to an angiotensin II peptide in a subject, which comprises

(I) the angiotensin II peptide consisting of the amino acid sequence of DRVYIHPF (SEQ ID NO: 21), and

(II) an expression vector encoding a chimeric hepatitis B virus core antigen polypeptide, into which the angiotensin II peptide of (I) has been inserted or added, wherein the angiotensin II peptide of (I) is inserted in a region of amino acid residues 74-87 or 130-138 of the hepatitis B virus core antigen polypeptide, or added to the N-terminal or C-terminal of the hepatitis B virus core antigen polypeptide,

wherein the angiotensin II peptide of (I) is cross-linked with a carrier protein, and

wherein the angiotensin II peptide of (I) and the expression vector of (II) are substantially simultaneously administered to the subject.

2. The combination according to claim 1 , wherein, in the chimeric hepatitis B virus core antigen polypeptide, the angiotensin II peptide of (I) is inserted between the amino acid residues 80 and 81 of the hepatitis B virus core antigen polypeptide.

3. The combination according to claim 1 , which is formulated as a single preparation.

4. The combination according to claim 1 , which is free of an adjuvant.

5. The combination according to claim 1 , which is for the treatment or prophylaxis of cardiac failure, hypertension, renal failure, arteriosclerosis, myocardial infarction, cerebral infarction, arteriosclerosis obliterans, or dementia.

6. The combination according to claim 5 , which is for the treatment or prophylaxis of cardiac failure caused by mitral insufficiency.

7. The combination according to claim 1 , wherein the subject is human or a non-human mammal.

8. A method of inducing a specific immune response to an angiotensin II peptide in a subject, which comprises substantially simultaneously administering to the subject one or more times:

(I) the angiotensin II peptide consisting of the amino acid sequence of DRVYIHPF (SEQ ID NO: 21), and

(II) an expression vector encoding a chimeric hepatitis B virus core antigen polypeptide, into which the angiotensin II peptide of (I) has been inserted or added,

wherein the angiotensin II peptide of (I) is inserted in a region of amino acid residues 74-87 or 130-138 of the hepatitis B virus core antigen polypeptide, or added to the N-terminal or C-terminal of the hepatitis B virus core antigen polypeptide, and

wherein the angiotensin II peptide of (I) is cross-linked with a carrier protein.

9. The method according to claim 8 , wherein the carrier protein is Keyhole Limpet Hemocyanin (KLH).

10. The method according to claim 8 , wherein the angiotensin II peptide of (I) and the expression vector of (II) are administered in a single dose.

11. The method according to claim 8 , wherein the angiotensin II peptide of (I) and the expression vector of (II) are administered by the same administration route.

12. The method according to claim 11 , wherein the angiotensin II peptide of (I) and the expression vector of (II) are administered subcutaneously, intradermally, or intramuscularly.

13. The method according to claim 8 , wherein electroporation and/or a nucleic acid introduction reagent are/is used for administration of the angiotensin II peptide of (I) and the expression vector of (II).

14. The combination according to claim 1 , wherein the carrier protein is KLH.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 9, 2023
From: SUMITOMO PHARMA ANIMAL HEALTH CO., LTD.
To: ANGES, INC.
Reel/Frame 063583/0482 →
CHANGE OF NAME Recorded May 17, 2022
From: DS PHARMA ANIMAL HEALTH CO., LTD.
To: SUMITOMO PHARMA ANIMAL HEALTH CO., LTD.
Reel/Frame 060101/0695 →
CHANGE OF NAME Recorded May 18, 2020
From: ANGES MG INC.
To: ANGES, INC.
Reel/Frame 052694/0198 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 24, 2018
From: NAKAGAMI, HIRONORI; MORISHITA, RYUICHI; KORIYAMA, HIROSHI; TOMIOKA, HIDEKI; NAOHARA, KENJI
To: ANGES MG, INC.; OSAKA UNIVERSITY; DS PHARMA ANIMAL HEALTH CO., LTD.
Reel/Frame 044717/0590 →
Priority Claims (1)
JP 2014-235736 · Nov 20, 2014 · national
Continuity (1)
Related Publication 20170258895A1 · Sep 14, 2017